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Journal Abstract Search

309 related items for PubMed ID: 7714085

  • 1. A new constitutively activating point mutation in the luteinizing hormone/choriogonadotropin receptor gene in cases of male-limited precocious puberty.
    Yano K, Saji M, Hidaka A, Moriya N, Okuno A, Kohn LD, Cutler GB.
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1162-8. PubMed ID: 7714085
    [Abstract] [Full Text] [Related]

  • 2. A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases.
    Yano K, Hidaka A, Saji M, Polymeropoulos MH, Okuno A, Kohn LD, Cutler GB.
    J Clin Endocrinol Metab; 1994 Dec; 79(6):1818-23. PubMed ID: 7527413
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  • 3. A case of male-limited precocious puberty caused by a point mutation in the second transmembrane domain of the luteinizing hormone choriogonadotropin receptor gene.
    Yano K, Kohn LD, Saji M, Kataoka N, Okuno A, Cutler GB.
    Biochem Biophys Res Commun; 1996 Mar 27; 220(3):1036-42. PubMed ID: 8607787
    [Abstract] [Full Text] [Related]

  • 4. Phe576 plays an important role in the secondary structure and intracellular signaling of the human luteinizing hormone/chorionic gonadotropin receptor.
    Yano K, Kohn LD, Saji M, Okuno A, Cutler GB.
    J Clin Endocrinol Metab; 1997 Aug 27; 82(8):2586-91. PubMed ID: 9253338
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  • 5. Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.
    Latronico AC, Shinozaki H, Guerra G, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL.
    J Clin Endocrinol Metab; 2000 Dec 27; 85(12):4799-805. PubMed ID: 11134146
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  • 6. A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty.
    Latronico AC, Abell AN, Arnhold IJ, Liu X, Lins TS, Brito VN, Billerbeck AE, Segaloff DL, Mendonca BB.
    J Clin Endocrinol Metab; 1998 Jul 27; 83(7):2435-40. PubMed ID: 9661624
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  • 7. [Constitutively activating mutations in the luteinizing hormone receptor gene in cases of male-limited precocious puberty].
    Yano K, Okuno A.
    Nihon Rinsho; 1998 Jul 27; 56(7):1843-7. PubMed ID: 9702063
    [Abstract] [Full Text] [Related]

  • 8. A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.
    Latronico AC, Anasti J, Arnhold IJ, Mendonça BB, Domenice S, Albano MC, Zachman K, Wajchenberg BL, Tsigos C.
    J Clin Endocrinol Metab; 1995 Aug 27; 80(8):2490-4. PubMed ID: 7629248
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  • 9. Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty.
    Nagasaki K, Katsumata N, Ogawa Y, Kikuchi T, Uchiyama M.
    Endocr J; 2010 Aug 27; 57(12):1055-60. PubMed ID: 21060208
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  • 11. A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.
    Shenker A, Laue L, Kosugi S, Merendino JJ, Minegishi T, Cutler GB.
    Nature; 1993 Oct 14; 365(6447):652-4. PubMed ID: 7692306
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  • 12. A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty.
    Kraaij R, Post M, Kremer H, Milgrom E, Epping W, Brunner HG, Grootegoed JA, Themmen AP.
    J Clin Endocrinol Metab; 1995 Nov 14; 80(11):3168-72. PubMed ID: 7593421
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  • 13. [Familial male-limited precocious puberty].
    Katsumata N, Tanaka T.
    Nihon Rinsho; 1997 Nov 14; 55(11):2959-62. PubMed ID: 9396295
    [Abstract] [Full Text] [Related]

  • 14. Thyrotropin, like luteinizing hormone (LH) and chorionic gonadotropin (CG), increases cAMP and inositol phosphate levels in cells with recombinant human LH/CG receptor.
    Hidaka A, Minegishi T, Kohn LD.
    Biochem Biophys Res Commun; 1993 Oct 15; 196(1):187-95. PubMed ID: 8216292
    [Abstract] [Full Text] [Related]

  • 15. A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty.
    Gromoll J, Partsch CJ, Simoni M, Nordhoff V, Sippell WG, Nieschlag E, Saxena BB.
    J Clin Endocrinol Metab; 1998 Feb 15; 83(2):476-80. PubMed ID: 9467560
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  • 16. Distinct mechanisms of cAMP induction by constitutively activating LH receptor and wild-type LH receptor activated by hCG.
    Lee C, Ji I, Ji TH.
    Endocrine; 2004 Nov 15; 25(2):111-5. PubMed ID: 15711023
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  • 18. [Analysis of a family affected with familial male-limited precocious puberty due to a Ala568Val mutation in LHCGR gene].
    Chen RM, Zhang Y, Yang XH, Lin XQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec 15; 29(6):631-4. PubMed ID: 23225038
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